Puja Merchant’s Post

#ICYMI: Watch our full webinar recording to explore how medical affairs is uniquely positioned to infuse drug development with the voice of the patient and bring scientific information with patient communities that benefit all: https://ow.ly/8BPp30sEVMZ #SyneosHealth

#ICYMI: Watch our full webinar recording to explore how medical affairs is uniquely positioned to infuse drug development with the voice of the patient and bring scientific information with patient communities that benefit all: https://ow.ly/zqZx30sF7ua #SyneosHealth

#ICYMI: Watch our full webinar recording to explore how medical affairs is uniquely positioned to infuse drug development with the voice of the patient and bring scientific information with patient communities that benefit all: https://ow.ly/FeTG30sEPzl #SyneosHealth

#ICYMI: Watch our full webinar recording to explore how medical affairs is uniquely positioned to infuse drug development with the voice of the patient and bring scientific information with patient communities that benefit all: https://ow.ly/uFTZ30sENUO #SyneosHealth

I think in 2024 we will see more technology changing how we do what we do. From AI generated content from curated input to technology enhancing the identification of insights. The big question is how to we harness the technology and make sure that the outputs are useful.

Let's hear it, Medical Information professionals: What are your predictions for 2024? One thing we do know: phactMI will continue to be the primary source for current, evidence-based drug information to support effective clinical decision making. #medicalinformation #druginformation

Join us for an insightful webinar based on #IQVIA's #LaunchExcellence research, which has analyzed over 1,000 new medical entity launches in the past 16 years. Discover the key challenges faced by launch teams post-pandemic and the critical role of #MedicalAffairs in overcoming these. https://bit.ly/3PaoMNs

Whether meeting FDA guidance, conducting comparator studies or researching new indications, real-world data can provide evidence of a treatment’s long-term safety and efficacy. Discover how HealthVerity FLOW can set you up for success, letting the data flow where you need it, when you need it and how you need it. https://hubs.ly/Q02q2dDY0

Unlock the Journey of Clinical Research! 🌐 Explore the world of clinical research in four phases: Phase 1 = safety and dosage, Phase 2 = efficacy and side effects, Phase 3 = confirmation, and regulatory approval! 📊 Join the vital work of bringing safe and effective treatments to patients worldwide. #ClinicalResearch #DrugDevelopment #MedicalInnovation #Healthcare"